Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_provenance.
- NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_assertion description "[This same region also contains genes for two of the structurally related factors, for c-kit, a receptor for an as yet unidentified ligand, and for 'piebald trait', an inherited skin pigmentation disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_provenance.
- NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_assertion evidence source_evidence_literature NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_provenance.
- NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_assertion SIO_000772 2970963 NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_provenance.
- NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_assertion wasDerivedFrom befree-20140225 NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_provenance.
- NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_assertion wasGeneratedBy ECO_0000203 NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP572484.RASyeRyVFjrQNset212N-_4FswrSzTdRLOK8xXi64vnMo130_provenance.